Universal Tracker Biopsy

GUDID 07540209955723

Universal Tracker Biopsy for use with Navient system, cranial

ClaroNav Kolahi Inc

Neurological stereotactic surgery system

• Primary Device ID: 07540209955723
• NIH Device Record Key: 8e4291a8-0766-42dc-abbc-6fbb6a938419
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Universal Tracker Biopsy
• Version Model Number: 950-NC-UTB
• Company DUNS: 203466065
• Company Name: ClaroNav Kolahi Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07540209955723 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241327

FDA Product Code

• HAW: Neurological Stereotaxic Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

[07540209955723]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-10
• Device Publish Date: 2025-02-28

Devices Manufactured by ClaroNav Kolahi Inc

• 07540209955501 - Navient System with kits: 2025-03-10 Navient System 955-NC-NC with kits
• 07540209955518 - Navient Accessory kit - cranial: 2025-03-10 Navient Accessory kit for use with Navient system, cranial
• 07540209955525 - Navient Accessory kit - biopsy: 2025-03-10 Navient Accessory kit - biopsy for use with Navient system, cranial
• 07540209955723 - Universal Tracker Biopsy: 2025-03-10Universal Tracker Biopsy for use with Navient system, cranial
• 07540209955723 - Universal Tracker Biopsy: 2025-03-10 Universal Tracker Biopsy for use with Navient system, cranial
• 07540209955730 - Universal Tracker Cusa: 2025-03-10 Universal Tracker Cusa for use with Navient system, cranial
• 07540209955747 - Universal Tracker Stimulation probe: 2025-03-10 Universal Tracker Stimulation probe for use with Navient system, cranial
• 07540209955754 - Universal Tracker Suction: 2025-03-10 Universal Tracker Suction for use with Navient system, cranial
• 07540209955945 - Navigated Shunt Needle: 2025-03-10 Navigated Shunt Needle for use with Navient system, cranial